MCID: GNT180
MIFTS: 3

Genetic Primary Hypomagnesemia with Normocalciuria

Categories: Metabolic diseases, Nephrological diseases, Rare diseases

Aliases & Classifications for Genetic Primary Hypomagnesemia with Normocalciuria

MalaCards integrated aliases for Genetic Primary Hypomagnesemia with Normocalciuria:

Name: Genetic Primary Hypomagnesemia with Normocalciuria 58

Classifications:

Orphanet: 58  
Rare renal diseases
Inborn errors of metabolism


External Ids:

ICD10 via Orphanet 33 E83.4
Orphanet 58 ORPHA306522

Summaries for Genetic Primary Hypomagnesemia with Normocalciuria

MalaCards based summary : Genetic Primary Hypomagnesemia with Normocalciuria

Related Diseases for Genetic Primary Hypomagnesemia with Normocalciuria

Symptoms & Phenotypes for Genetic Primary Hypomagnesemia with Normocalciuria

Drugs & Therapeutics for Genetic Primary Hypomagnesemia with Normocalciuria

Search Clinical Trials , NIH Clinical Center for Genetic Primary Hypomagnesemia with Normocalciuria

Genetic Tests for Genetic Primary Hypomagnesemia with Normocalciuria

Anatomical Context for Genetic Primary Hypomagnesemia with Normocalciuria

Publications for Genetic Primary Hypomagnesemia with Normocalciuria

Variations for Genetic Primary Hypomagnesemia with Normocalciuria

Expression for Genetic Primary Hypomagnesemia with Normocalciuria

Search GEO for disease gene expression data for Genetic Primary Hypomagnesemia with Normocalciuria.

Pathways for Genetic Primary Hypomagnesemia with Normocalciuria

GO Terms for Genetic Primary Hypomagnesemia with Normocalciuria

Sources for Genetic Primary Hypomagnesemia with Normocalciuria

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Apr-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 Tocris
70 UMLS
71 UMLS via Orphanet
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